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ChemInform Abstract: α‐Lithiation—Electrophile Trapping of N‐Thiopivaloylazetidin‐3‐ol: Stereoselective Synthesis of 2‐Substituted 3‐Hydroxyazetidines.

David M. Hodgson, Christopher I. Pearson, Amber L. Thompson

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Abstract

Abstract Treatment of the azetidinol (I) with sBuLi followed by reaction with various electrophiles results in stereoselective formation of 2,3‐trans‐substituted derivatives with exception of CD3OD which predominantly yields the cis‐product.

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What this paper is about

Abstract Treatment of the azetidinol (I) with sBuLi followed by reaction with various electrophiles results in stereoselective formation of 2,3‐trans‐substituted derivatives with exception of CD3OD which predominantly yields the cis‐product.

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Available abstract

Abstract Treatment of the azetidinol (I) with sBuLi followed by reaction with various electrophiles results in stereoselective formation of 2,3‐trans‐substituted derivatives with exception of CD3OD which predominantly yields the cis‐product.

Key concepts: Chemistry, Stereoselectivity, Electrophile, Trapping, Medicinal chemistry, Combinatorial chemistry, Stereochemistry, Organic chemistry

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ChemInform Abstract: α‐Lithiation—Electrophile Trapping of N‐Thiopivaloylazetidin‐3‐ol: Stereoselective Synthesis of 2‐Substituted 3‐Hydroxyazetidines. — Research Paper | ScholarLens